临床运营专员/高级 - 英国 - 客户专属
Clinical Operations Specialist/Sr - UK - Sponsor-dedicated
临床运营专员/高级专员 - 英国 - 客户专属
Syneos Health® 是一家领先的全面整合的生物制药解决方案组织,旨在加速客户成功。我们将独特的临床、医学事务和商业洞察转化为成果,以应对现代市场现实。
我们的临床开发模式将客户和患者置于我们所做一切的核心。我们不断寻找简化和优化工作的方法,不仅使 Syneos Health 更容易合作,也使我们更容易被雇佣。
无论您加入我们作为功能服务提供商合作伙伴还是全服务环境,您都将与充满热情的问题解决者合作,作为团队进行创新,帮助客户实现目标。我们敏捷且有动力加速疗法的交付,因为我们热衷于改变生命。
了解我们的 29,000 名员工,他们在 110 个国家已经知道:
在这里工作,处处重要
为什么选择 Syneos Health
- 我们致力于通过职业发展和晋升来培养员工;提供支持性和参与度高的直线管理;技术及治疗领域培训;同行认可和全面奖励计划。
- 我们致力于打造 Total Self 文化——在这里你可以真实地做自己。我们的 Total Self 文化将我们全球的员工团结在一起,我们致力于照顾好我们的员工。
- 我们持续打造我们所有人都想工作的公司,也是客户想合作的公司。为什么?因为当我们将思想、背景、文化和观点的多样性汇聚在一起时,我们能够创造一个让每个人感到归属感的环境。
职位职责
- 确保临床研究项目的安全和有效运作,包括实施先进的方法和技术以提高研究结果
- 在医疗层面保障研究受试者的福祉,确保遵守伦理标准和患者护理的最佳实践
- 审查研究方案并按照方案和监管、健康及安全标准执行程序,包括制定风险缓解策略和合规性监控
- 在必要时提出或升级研究问题,提供详细的分析和解决建议
- 招募并协调与临床试验志愿者和患者的沟通,利用创新的招募策略并保持清晰的沟通
查看英文原文
Clinical Operations Specialist/Sr - UK - Sponsor-dedicatedSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job Responsibilities
- Ensure safe and effective operations of clinical research studies, including the implementation of advanced methodologies and technologies to enhance study outcomes
- Safeguard the wellbeing of research subjects in a medical capacity, ensuring adherence to ethical standards and best practices in patient care
- Review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards, including the development of risk mitigation strategies and compliance monitoring
- Raise or escalate study issues as necessary, providing detailed analysis and recommendations for resolution
- Recruit and coordinate communication with clinical trial volunteers and patients, utilizing innovative recruitment strategies and maintaining clear and consistent communication throughout the study
- Follow applicable regulations globally and by region, ensuring all activities are compliant with local and international guidelines
- Collaborate with cross-functional teams to develop study materials, including the creation of comprehensive training programs and resources for study personnel
- Monitor trial progress and address any issues that arise during the study, employing data-driven approaches to identify and resolve challenges promptly
Qualifications:
- Established and experienced support individual contributor; this role is a progression within the level from a Clin Ops Specialist
- Broad knowledge of operational systems and practices typically gained through extensive experience and/or education
Certifications:
· Relevant certifications in clinical operations or related field
Necessary Skills:
- Strong organizational and communication skills
- Ability to work under supervision and follow established protocols
- Attention to detail and ability to handle routine tasks with some deviation from standard practice
- Ability to collaborate effectively with cross-functional teams
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Originally posted on Himalayas